PSI-6130
CAS No. 817204-33-4
PSI-6130 ( PSI6130 | R-1656 | R1656 )
产品货号. M16043 CAS No. 817204-33-4
一种有效的、特异性的 HCV RNA 合成抑制剂,通过抑制 NS5B RNA 聚合酶(复制子测定中 EC90=4.6 uM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥1077 | 有现货 |
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5MG | ¥1458 | 有现货 |
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10MG | ¥2333 | 有现货 |
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25MG | ¥3929 | 有现货 |
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50MG | ¥5613 | 有现货 |
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100MG | ¥7995 | 有现货 |
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500MG | ¥15957 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称PSI-6130
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种有效的、特异性的 HCV RNA 合成抑制剂,通过抑制 NS5B RNA 聚合酶(复制子测定中 EC90=4.6 uM)。
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产品描述A potent, specific inhibitor of HCV RNA synthesis by inhibiting the NS5B RNA polymerase (EC90=4.6 uM in replicon assay); shows no anti-BVDV activity and weak antiviral activity against other flaviviruses, including West Nile virus, Dengue type 2, and yellow fever virus; has little or no cytotoxicity against various cell type.HCV Infection Discontinued.
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体外实验PSI-6130 exhibits potent and specific inhibitory activity against HCV RNA replication mediated by the NS5B polymerase. Both PSI-6130 inhibit HCV GT-1b (Con1 strain) and GT-1a (H77 strain) subgenomic RNA replication, with mean EC50 values of 0.51 and 0.30 μM, respectively. PSI-6130 inhibits 40% human serum with EC50 of 0.51 μM. PSI-6130 inhibits HCV replication with a mean IC50 of 0.6 μM, PSI-6130-TP inhibits HCV replicase with a mean IC50 of 0.34 μM. PSI-6130-TP inhibits recombinant HCV Con1 NS5B on a heteropolymeric RNA template derived from the 3′-end of the negative strand of the HCV genome with an IC50 of 0.13 μM and Ki of 0.023 μM.
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体内实验——
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同义词PSI6130 | R-1656 | R1656
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通路Microbiology/Virology
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靶点HCV
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受体HCV
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研究领域Infection
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适应症HCV Infection
化学信息
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CAS Number817204-33-4
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分子量259.2343
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分子式C10H14FN3O4
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESOC[C@@H]1[C@H]([C@](C)(F)[C@H](N2C(N=C(C=C2)N)=O)O1)O
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化学全称Cytidine, 2'-deoxy-2'-fluoro-2'-methyl-, (2'R)-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Clark JL, et al. J Med Chem. 2005 Aug 25;48(17):5504-8.
2. Murakami E, et al. Antimicrob Agents Chemother. 2007 Feb;51(2):503-9.
3. Stuyver LJ, et al. Antivir Chem Chemother. 2006;17(2):79-87.
4. Ma H, et al. J Biol Chem. 2007 Oct 12;282(41):29812-20.